Methods for fixing and detecting RNA

a technology of fixing and detecting rna, applied in the direction of microbiological testing/measurement, biochemistry apparatus and processes, screening process, etc., can solve the problem that current ish are not reliable for measuring small nucleic acids

Active Publication Date: 2016-06-07
THE ROCKEFELLER UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

RNA impacts nearly every aspect of gene expression and many human diseases are caused by or result in mistakes in RNA metabolism, e.g. mutations in pre-mRNAs lead to splicing defects or degradation of mRNAs by trigger nonsense-mediated mRNA decay.
As a consequence, current ISH are not reliable for measuring small nucleic acids such as miRNA.

Method used

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Examples

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Effect test

example 1

[0209]To assess miRNA expression differences between tumors, total RNA was extracted from 36 archived clinical materials and fresh cell lines from patients with Merkel cell carcinoma (MCC), basal cell carcinoma (BCC), and normal skin (NS) (FIG. 16).

[0210]We subsequently profiled and quantitated miRNAs in all samples using barcoded small RNA sequencing. Sequence reads were annotated by RNA category (FIG. 17). Total miRNA concentrations were calculated for all samples using sequence read and RNA input ratios and averaged 11.6 (range: 4.6-41.7) fmol / μg (FIG. 18). Higher total miRNA concentrations were seen in Trizol-extracted fresh cell lines (CL) compared to Masterpure- or RecoverAll-extracted FFPE samples (FIG. 4), consistent with reported differences arising from sample processing and / or RNA extraction method. To minimize these differences, we compared concentrations in RecoverAll-extracted FFPE samples from sequencing run one (hereafter termed the training set). Total miRNA concent...

example 2

[0224]miRNAs are valuable disease biomarkers because of their cell-type specificity and abundance. We developed barcoded small RNA sequencing for simultaneous miRNA profiling and quantitation in multiple samples. Through profiling and discriminant analysis, we identified a distinct, inverse relationship between miR-205 and miR-375 expression that differentiated two skin tumors with shared histologic features, namely basal cell carcinoma (BCC) and Merkel cell carcinoma (MCC).

[0225]We designed probes targeting these tumor-specific biomarkers and rRNA to establish multicolor miRNA fluorescence in situ hybridization (FISH) on formalin-fixed paraffin-embedded (FFPE) tissue sections. Amplified miRNA signals were corrected and normalized against directly detectable reference rRNA signals and tumor-specific cut-off values were established. We subsequently validated our method on 16 BCC and MCC tumors, correctly identifying all tumors in a blinded analysis. Parallel visualization of differen...

example 3

[0243]We demonstrate the use of specifically designed LNA-modified DNA (LNA / DNA) probes. FIG. 45 shows comparison of LNA / DNA probes to DNA probes of various length. Here, we show how important it is to have short LNA / DNA probes to get desired specificity. For example, to target HER2 / ERBB2, we synthesized 45 DNA probes (24-30 nt long), which were designed with GC content between 50 and 64% and TC content between 45 and 66%. No special care was taken regarding probes mishybridization to rRNA. Melting temperatures of these DNA probes varied from 48.1 to 56.9° C. rRNA mishybridization of DNA probes dominated the signal indicating that these DNA probes are not specific (FIG. 45a). Subsequently, DNA probes (24-30 nt long) were shorten either from 5′-end or 3′-end to avoid rRNA mishybridization (no segment longer than 8 nt with rRNA sequence complementarity) to yield 39 shorter DNA probes (14-21 nt long). Melting temperatures of these DNA probes varied from 38.8 to 47.1° C. (approximately ...

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Abstract

The invention provides a method for fixing an RNA molecule in a biological sample. The method comprises contacting the biological sample with an aldehyde-containing fixative, and subsequently contacting the sample with a solution comprising a carbodiimide and a heterocyclic derivative selected from the group consisting of an imidazole, pyrazole, triazole or tetrazole or a combination thereof. A method for differentiating cells in a biological sample is also provided. A method for quantification of RNA retention in a biological sample is also provided. A kit for fixing RNA in a sample is provided as well.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a U.S. National Phase Application of International Application No. PCT / US2012 / 048727 filed on Jul. 27, 2012 and asserts priority to U.S. Provisional Patent Application No. 61 / 512,228 filed on Jul. 27, 2011, all of which are hereby incorporated by reference in their entirety.[0002]This application claims priority to U.S. Provisional Application No. 61 / 512,228 filed Jul. 27, 2011.[0003]This invention was made with government support under NCI RO1 CA159227-01 awarded by the National Institutes of Health. Accordingly, the government has certain rights in the invention.BACKGROUND OF THE INVENTION[0004]RNA impacts nearly every aspect of gene expression and many human diseases are caused by or result in mistakes in RNA metabolism, e.g. mutations in pre-mRNAs lead to splicing defects or degradation of mRNAs by trigger nonsense-mediated mRNA decay. It has been shown that in addition to RNA's fundamental roles in information tra...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): C12Q1/68G01N1/30C12N15/11
CPCC12Q1/6806C12N15/111G01N1/30C12N2310/141C12N2320/10C12Q2600/178
Inventor TUSCHL, THOMASCEKAN, PAVOLRENWICK, NEIL
Owner THE ROCKEFELLER UNIV
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